Novel and effective hemostats based on graphene oxide-polymer aerogels: <i>In vitro</i> and<i> in vivo</i> evaluation
Abstract
In this study, graphene oxide (GO)-based aerogels cross-linked with chitosan (CS), gelatin (GEL), and polyvinyl alcohol (PVA) were characterized and their hemostatic efficiencies both in vitro and in vivo were investigated and compared to commercial materials (ChitoGauze??XR and SpongostanTM). All aerogels exhibited highly porous structures and a negative surface charge density favorable to their interaction with blood cells. The in vitro studies showed that all aerogels coagulated 60 % of the blood contained in their structures after 240 s of the whole-blood clotting assay, the GO-CS aerogel being the one with the highest blood clotting. All aerogels showed high hemocompatibility, with hemolytic rates <5 %, indicating their use as biomaterials. Among them, the GOGEL aerogel exhibited the lowest hemolytic activity, due possibly to its high GEL content compared to the GO amount. According to their blood clotting activity, aerogels did not promote coagulation through extrinsic and intrinsic pathways. However, their surfaces are suitable for accelerating hemostasis by promoting alternative routes. All aerogels adhered platelets and gathered RBCs on their surfaces, and in addition the GO-CS aerogel surface also promoted the formation of filamentous fibrin networks adhered on its structure. Furthermore, in vivo evaluations revealed that all aerogels significantly shortened the hemostatic times and reduced the blood loss amounts compared both to the SpongostanTM and ChitoGauze??XR commercial materials and to the gauze sponge (control group). The hemostatic performance in vitro and in vivo of these aerogels suggests that they could be used as hemostats for controlling profuse bleedings.
Más información
Título según WOS: | Novel and effective hemostats based on graphene oxide-polymer aerogels: In vitro and in vivo evaluation |
Título según SCOPUS: | ID SCOPUS_ID:85133492683 Not found in local SCOPUS DB |
Volumen: | 139 |
Fecha de publicación: | 2022 |
DOI: |
10.1016/J.BIOADV.2022.213007 |
Notas: | ISI, SCOPUS |